Identity
- Trade Name
- VitreQ FDA UDI
- Generic Name
- Intraocular scissors, probe-like, single-use FDA UDI
- Device Name
- 25G Scissors, Horizontal Curved FDA UDI
- Model / Reference
- SC25.D03 FDA UDI
- Description
- 25G Scissors, Horizontal Curved FDA UDI
Identifiers
- Primary DI / UDI-DI
- 88719214220439 FDA UDI
- FDA Product Code
- HNF FDA UDI
- GMDN Term
- Intraocular scissors, probe-like, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Intraocular scissors, probe-like, single-use
VitreQ by Vitreq B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intraocular scissors, probe-like, single-use.
- 27ga Dex™ Curved Horizontal Scissors — KATALYST SURGICAL, LLC · Class I
- 25ga DEX Stiff Vertical Scissors — KATALYST SURGICAL, LLC · Class I
- Disposable Microscissors: Hooked. (27 gauge / 0.4 mm) — D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Class I
- 25ga DEX Stiff Curved Horizontal Scissors — KATALYST SURGICAL, LLC · Class I
- 23ga Dex™ Curved Horizontal Scissors — KATALYST SURGICAL, LLC · Class I
- Disposable Microscissors: Curved, Horizontal.(20 gauge / 0.9 mm) — D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Class I
- Disposable Microscissors: Curved, Horizontal.(25 gauge / 0.5 mm) — D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Class I
- 25ga Dex™ Curved Horizontal Scissors — KATALYST SURGICAL, LLC · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Vitreq B.V.
Sources (1)
- FDA UDI a30b4215-f11f-4260-9ed7-b0b6ab9682bd 34 fields · synced May 30, 2026